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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45574생성일: 2026년 10월 24일

Ammonia → 2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt)

https://huagongshe.com/ko/reaction/45574

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Sodium IodideHCID 5238—
반응물Benzenesulfonic AcidHCID 7371—
반응물2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonateHCID 58249642—
용매Dimethyl SulfoxideHCID 679—
용매Isopropyl AcetateHCID 7915—
생성물2,2-difluoro-2-pyridin-2-yl-ethylamine benzenesulphonate, (1:1 salt)HCID 7835786349.5%

반응 조건

온도80 °C

반응 단계

10 g of 2,2-Difluoro-2-pyridin-2-ylethyl 4-methylbenzenesulfonate (J) obtained in step 3, 5 g of NaI, 20 mL of DMSO and 90 mL of aqueous ammonia were taken in a 500 mL autoclave vessel. The reaction mixture was heated to 80° C. and a pressure of 15 to 17 kg of ammonia maintained for 30-40 hours. The volume of the reaction mass was reduced by vacuum distillation. The RM was washed with 60 mL of IPE. The pH of the RM was adjusted to 10-14 by adding a 50% NaOH solution and extracted three times with 60 mL of MDC. The combined MDC layers were washed with brine, dried over sodium sulphate and distilled under vacuum (crude weight=8 g). The crude mass obtained was dissolved with 10 mL of MDC, and to this 4.5 g benzene sulphonic acid (BSA) dissolved in 30 mL isopropyl acetate (IPAc) was added dropwise over a period of 30 minutes with stirring at RT. The RM was stirred for 30 minutes at RT. The solid obtained was filtered and washed with IPAc and dried under vacuum, resulting in 5 g of the titled compound (Yield=49.5%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541580B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-ac1aafe395f44b6fa336ed0ef1904144
출처 메모uspto-grants-2013_09